Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:27573430-27573535 | Common:5; Rare:58 | ||||
chr9:32573078-32573207 | Common:2; Rare:49 | ||||
chr9:33001536-33001721 | Common:2; Rare:102; Clinvar (benign):4 | ||||
chr9:33025066-33025383 | Common:7; Rare:129 | ||||
chr9:33076611-33076865 | Common:2; Rare:88 | ||||
chr9:33166880-33166994 | Rare:47 | ||||
chr9:33290405-33290575 | Common:2; Rare:67 | ||||
chr9:33473843-33474144 | Common:4; Rare:93 | ||||
chr9:34048857-34048973 | Rare:47 | ||||
chr9:34049164-34049224 | Rare:18 | ||||
chr9:34178938-34179090 | Common:1; Rare:42 | ||||
chr9:34179250-34179398 | Rare:27 | ||||
chr9:34329195-34329638 | Common:1; Rare:138 | ||||
chr9:34458536-34458826 | Rare:68 | ||||
chr9:34612079-34612183 | Common:2; Rare:34 |